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NCT00628251 · MORE INFO

Limitations, agreements, and source contact

Dose-finding Study Comparing Efficacy and Safety of a PARP Inhibitor Against Doxil in BRCA+ve Advanced Ovarian Cancer · Source last updated 2019-12-05

Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.

certain Agreement
other Details
No publication of the study results may be made until publication of the results of the multi-centre study or 2 years after study completion, whichever is the sooner
pi Sponsor Employee
false
restriction Type
OTHER
restrictive Agreement
true
limitations And Caveats
description
The AEs reported include all events up to the OS data cut-off. After the PFS data cut-off, AEs were only collected for the olaparib and cross-over groups. The safety profile of these 2 groups at OS was consistent with that at the time of PFS.
point Of Contact
email
ClinicalTrialTransparency@astrazeneca.com
organization
AstraZeneca
phone
+44 7884 735492
title
Paula del Rosario
Complete source fields
certain Agreement
other Details
No publication of the study results may be made until publication of the results of the multi-centre study or 2 years after study completion, whichever is the sooner
pi Sponsor Employee
false
restriction Type
OTHER
restrictive Agreement
true
limitations And Caveats
description
The AEs reported include all events up to the OS data cut-off. After the PFS data cut-off, AEs were only collected for the olaparib and cross-over groups. The safety profile of these 2 groups at OS was consistent with that at the time of PFS.
point Of Contact
email
ClinicalTrialTransparency@astrazeneca.com
organization
AstraZeneca
phone
+44 7884 735492
title
Paula del Rosario

Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0

Preserved source evidence · Not medical advice